U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 114

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098884copy number variation1nstd102humanPathogenic GRCh37 chr6: 82,828,591-86,578,811 , GRCh38.p12 chr6: 82,118,874-85,869,093 LOC105377879, LOC100421583, 47 more genes
    nsv6791212copy number variation1nstd229human GRCh38 chr6: 77,944,413-86,852,671 , GRCh37.p13 chr6: 78,654,130-87,562,389 SH3BGRL2, LCAL1, 93 more genes
    nsv6636874copy number variation1nstd102humanUncertain significance GRCh37 chr6: 81,087,736-84,200,632 , GRCh38.p12 chr6: 80,378,019-83,490,913 PGM3, ME1, 24 more genes
    nsv6634392copy number variation1nstd102humanUncertain significance GRCh37 chr6: 78,911,022-98,909,173 , GRCh38.p12 chr6: 78,201,305-98,461,297 MTHFD2P2, RPL7P27, 212 more genes
    nsv6405981copy number variation1nstd223human GRCh38 chr6: 83,191,902-83,192,327 , GRCh37.p13 chr6: 83,901,621-83,902,046 PGM3, RWDD2A
    nsv6399260copy number variation1nstd223human GRCh38 chr6: 83,108,063-83,419,637 , GRCh37.p13 chr6: 83,817,782-84,129,356 ME1, PGM3, 2 more genes
    nsv6313857copy number variation1nstd102humanPathogenic GRCh37 chr6: 69,938,252-94,379,210 , GRCh38.p12 chr6: 69,228,360-93,669,492 LOC101928570, RNU4-72P, 288 more genes
    nsv6313843copy number variation1nstd102humanUncertain significance GRCh37 chr6: 83,888,683-83,941,662 , GRCh38.p12 chr6: 83,178,964-83,231,943 RWDD2A, PGM3, 1 more genes
    nsv6290989copy number variation1nstd102humanPathogenic GRCh37 chr6: 83,141,523-88,023,466 , GRCh38.p12 chr6: 82,431,806-87,313,748 KRT18P30, LOC107986620, 58 more genes
    nsv6135853copy number variation1nstd213human GRCh37 chr6: 83,000,000-84,160,001 , GRCh38.p12 chr6: 82,290,283-83,450,282 ME1, PGM3, 8 more genes
    nsv5455139copy number variation1nstd206human GRCh38 chr6: 83,191,861-83,192,156 , GRCh37.p13 chr6: 83,901,580-83,901,875 PGM3, RWDD2A
    nsv5381391copy number variation1nstd102humanUncertain significance GRCh37 chr6: 83,878,953-84,567,108 , GRCh38.p12 chr6: 83,169,234-83,857,389 DOP1A, LOC105377879, 6 more genes
    nsv5369371translocation1nstd200human GRCh38 chr6: 83,191,890-83,191,890 , GRCh38 chr6: 83,192,136-83,192,136 , GRCh37.p13 chr6: 83,901,855-83,901,855 , GRCh37.p13 chr6: 83,901,609-83,901,609 RWDD2A, PGM3
    nsv5337374translocation1nstd200human GRCh37 chr6: 83,901,855-83,901,855 , GRCh37 chr6: 83,901,609-83,901,609 , GRCh38.p12 chr6: 83,191,890-83,191,890 , GRCh38.p12 chr6: 83,192,136-83,192,136 RWDD2A, PGM3
    nsv5315135copy number variation1nstd204human GRCh37.p13 chr6: 83,751,730-83,906,773 , GRCh38.p13 chr6: 83,042,011-83,197,054 PGM3, DOP1A, 2 more genes
    nsv5235293copy number variation1nstd204human GRCh38.p13 chr6: 83,193,242-83,194,241 , GRCh37.p13 chr6: 83,902,961-83,903,960 PGM3, RWDD2A
    nsv4941868copy number variation1nstd200human GRCh38 chr6: 83,089,224-83,341,439 , GRCh37.p13 chr6: 83,798,943-84,051,158 ME1, PGM3, 2 more genes
    nsv4816776copy number variation1nstd200human GRCh37 chr6: 83,751,736-83,906,764 , GRCh38.p12 chr6: 83,042,017-83,197,045 PGM3, RWDD2A, 2 more genes
    nsv4675056copy number variation1nstd102humanUncertain significance GRCh37 chr6: 82,620,262-84,201,117 , GRCh38.p12 chr6: 81,910,545-83,491,398 LOC100132659, DOP1A, 14 more genes
    nsv4607045copy number variation1nstd183human GRCh37 chr6: 83,903,097-83,903,173 , GRCh38.p12 chr6: 83,193,378-83,193,454 RWDD2A, PGM3
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center